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The Treatment of a Novel Epidermal Growth Factor Receptor (EGFR)-GRB2 Genetic Mutation Using Osimertinib in
Siddharth Ramanathan1, Nathan Shen2, Larry Kestin3
1College of Medicine, Oakland University William Beaumont School of Medicine, Rochester Hills, USA.
Abstract:
Mutations in the epidermal growth factor receptor (EGFR) have been implicated in nearly one-third of non-small-cell lung cancers. For patients harboring non-traditional mutations, genomic and transcriptomic sequencing can help direct treatment. As cancer genomics evolves, novel driver mutations continue to be uncovered. We report on a unique EGFR-GRB2 fusion in a 48-year-old female never-smoker. This patient presented with stage IV lung adenocarcinoma (T2aN3M1) with metastatic disease in the iliac wing and liver. Despite systemic treatment, this patient continued to progress. On whole transcriptome sequencing, this patient was found to have a novel EGFR-GRB2 RNA fusion transcript similar to other EGFR fusions described in the literature. After treatment with osimertinib, this patient experienced remarkable clinical and radiological improvements. We believe that, especially for patients with metastatic lung cancer, the presence of novel driver mutations should be investigated. Potentially, patients harboring similar mutations may demonstrate analogous improvements with targeted treatment using the most recent generation of tyrosine kinase inhibitors.
Insights
A novel epidermal growth factor receptor (EGFR) fusion with GRB2 was identified in a patient with advanced lung cancer. Targeted therapy with osimertinib led to significant clinical improvement, highlighting the importance of investigating rare mutations.
Area of Science:
- Oncology
- Genomics
- Molecular Biology
Background:
- Epidermal growth factor receptor (EGFR) mutations are common in non-small-cell lung cancer (NSCLC).
- Genomic and transcriptomic sequencing are crucial for identifying non-traditional mutations in NSCLC.
- The discovery of novel driver mutations is an ongoing area of cancer genomics research.
Observation:
- A unique EGFR-GRB2 fusion transcript was identified in a 48-year-old female never-smoker with stage IV lung adenocarcinoma.
- The patient had metastatic disease to the iliac wing and liver and progressed despite systemic treatment.
Findings:
- Whole transcriptome sequencing revealed a novel EGFR-GRB2 RNA fusion.
- Treatment with osimertinib resulted in remarkable clinical and radiological improvements for the patient.
Implications:
- Investigating novel driver mutations is essential, particularly in patients with metastatic lung cancer.
- Patients with similar rare mutations may benefit from targeted therapies like third-generation tyrosine kinase inhibitors.
- This case underscores the potential of precision medicine in treating NSCLC with uncommon genomic alterations.
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